Indian Journal of Dermatology
CASE REPORT
Year
: 2018  |  Volume : 63  |  Issue : 2  |  Page : 172--175

A tale of H syndrome with typical radiographic findings


Praneet Pradeep Awake1, Lakshmi Chandravathi Penmetcha1, Anil Fonseca2, Prasad Prabhakar Jawalkar3,  
1 Department of Dermatology, Venereology and Leprosy, Care Institute of Medical Sciences, Hyderabad, Telangana, India
2 Department of Pathology, Care Institute of Medical Sciences, Hyderabad, Telangana, India
3 Department of Radiology, Yashoda Hospital, Hyderabad, Telangana, India

Correspondence Address:
Dr. Praneet Pradeep Awake
Department of Dermatology, Venereology and Leprosy, Care Institute of Medical Sciences, Road No. 1, Banjara Hills, Hyderabad - 500 034, Telangana
India

Abstract

H syndrome is a recently described autosomal recessive genodermatosis with cutaneous phenotypes of varying severity and multi-system involvement. Patients suffering from this disorder can be easily mistaken for sclerodermoid conditions. The radiological findings of H syndrome are typical but have been described only anecdotally. We present a case of a 29 year old male patient of H syndrome with typical radiological features.



How to cite this article:
Awake PP, Penmetcha LC, Fonseca A, Jawalkar PP. A tale of H syndrome with typical radiographic findings.Indian J Dermatol 2018;63:172-175


How to cite this URL:
Awake PP, Penmetcha LC, Fonseca A, Jawalkar PP. A tale of H syndrome with typical radiographic findings. Indian J Dermatol [serial online] 2018 [cited 2022 May 20 ];63:172-175
Available from: https://www.e-ijd.org/text.asp?2018/63/2/172/229451


Full Text

 Introduction



H syndrome is an autosomal recessive genodermatosis, first described in 2008.[1] It has multisystemic involvement and is characterized by numerous clinical features, including cutaneous hyperpigmentation and hypertrichosis, hepatosplenomegaly, hearing loss, heart anomalies, hypogonadism, low height (short stature), hyperglycemia (insulin-dependent diabetes mellitus), and hallux valgus/flexion contractures.[1],[2] Cutaneous hyperpigmentation, commonly accompanied by hypertrichosis and progressive sclerodermatous induration, typically affecting initially the medial thighs with sparing of the knees, is the hallmark of the disorder and is considered pathognomonic.[2]

 Case Report



A 29-year-old male patient presented with a 6-year history of asymptomatic progressive cutaneous sclerosis, hyperpigmentation, and hypertrichosis over both thighs and trunk.

He complained of skin tightness around the abdomen while walking. He wandered to and fro between different specialists but without much help. He was diagnosed as Type 1 diabetic 6 years back and was receiving insulin since then.

Cutaneous examination revealed large ill-defined hyperpigmented indurated plaques extending symmetrically from mid-truncal area to both thighs characteristically sparing the knees and medial aspect of buttocks [Figure 1]a and [Figure 1]b. A prominent constriction band was noted around the abdomen [Figure 2]. The lesions over thighs were associated with hypertrichosis and were warm to touch.{Figure 1}{Figure 2}

Examination also revealed short stature (145 cm), hypospadias, micropenis, scrotal swelling, and mild hepatomegaly and inguinal lymphadenopathy. Axillary and pubic hairs were scanty. Other secondary sexual characters such as facial hair were sparse and voice was normal. Nails and teeth were normal. Ophthalmologic and auditory examinations were normal. On the basis of cutaneous findings, we kept differential diagnosis of morphea profunda, pseudoscleroderma, POEMS syndrome, Rosai–Dorfman syndrome, pigmented hypertrichotic dermatosis, and scleredema as the possibilities.

A deep skin biopsy was done from the indurated plaque on the lateral part of the left thigh and sent for histopathology. Skin biopsy revealed marked fibrosis of the dermis and subcutaneous tissue [Figure 3]a. Dermal appendages pushed upward, and a perivascular infiltrate of lymphocytes and histiocytes with foamy cytoplasm were seen intermingled with the bundles of dermal collagen. Septal panniculitis with plasma cell infiltration was noted [Figure 3]b. Histopathology report suggested sclerodermatous changes with immunostain CD68+ve histiocytes [Figure 3]c.{Figure 3}

Routine laboratory investigations revealed a fasting blood glucose level of 250 mg/dL and random blood sugar of 338 mg/dL with glycated hemoglobin 10.2%. Thyroid profile, liver function, kidney function, serum testosterone, follicle stimulating hormone and luteinizing hormone levels were normal. Antinuclear antibody was negative. Ultrasound abdomen revealed mild hepatosplenomegaly and abdominal lymphadenopathy. Color Doppler study of the scrotal region revealed small penis, normal echotexture, no calcific plaques, and small left testis. Chest radiography and nerve conduction studies were normal.

Computed tomography (CT) demonstrated marked symmetrical thickening of the skin with infiltration of subcutaneous tissue at the lower half of the body from infraumbilical region till scrotum and into bilateral gluteal region down to the knees [Figure 4]a and [Figure 4]b. Para-aortic and inguinal lymphadenopathy [Figure 5] and mild pericardial effusion [Figure 6] were noted. Marked thickening of the scrotum was seen [Figure 7]. A diagnosis of “H syndrome” was made. Genetic testing was not possible due to resource constraints.{Figure 4}{Figure 5}{Figure 6}{Figure 7}

 Discussion



The name H syndrome was first coined by Molho-Pessach et al.[1] It is recently described as an autosomal recessive disorder characterized by unique progressive symmetrical cutaneous induration with hyperpigmentation and hypertrichosis, localized mainly to the lower half of the body, hepatosplenomegaly, hearing loss, low height, hyperglycemia/diabetes mellitus, heart anomalies, hypogonadism, and hallux valgus/flexion contractures.[2] Other features include massive lymphadenopathy, pancreatic exocrine insufficiency, renal abnormalities, bone sclerosis, lytic bone lesions, swollen respiratory mucosa, infiltrated cheeks, and recurrent fever.[1],[2],[3]

It occurs due to biallelic mutations in SLC29A3 gene encoding the human equilibrative nucleoside transporter 3. SLC29A3 gene is widely expressed in various organs and regulates the inflammatory cascade.[2] A defect in this protein causes disordered immune regulation inflammatory infiltrates in the skin and internal organs. Failure to suppress the inflammation finally results in fibrosis.[4]

The pathognomonic finding is the cutaneous feature seen in 68% of patients and tends to appear during the first or second decade of life, initially over the inner thighs, spreading later to involve other areas.[1],[2],[5] Histopathological examination of affected skin demonstrates widespread dermal and subcutaneous fibrosis with a mononuclear infiltrate composed mainly of CD68+ histiocytes and plasma cells.[6] This feature implies that H syndrome is a novel form of inherited histiocytosis.

The radiographic findings of H syndrome are typical. Hiller N et al. described the spectrum of radiological findings in 12 patients with H syndrome in a recent study.[7] In majority of them, a typical and unique pattern of diffuse symmetric infiltration of the subcutaneous fat in the lower half of the body, with varying degrees of severity, was demonstrated. Changes in subcutaneous fat were accompanied by thickening of the skin, and in severe cases, cutaneous and subcutaneous changes lead to retraction of the underdeveloped external genitalia (micropenis) as were noticed in our case. The degree of subcutaneous thickening is related to patient's age, with older patients showing more severe infiltration of the subcutaneous tissue.[7]

Several conditions are characterized by radiological findings of dermal and subcutaneous changes similar to those seen in H syndrome.[8] The major disorder considered in the differential diagnosis is morphea and plasma cell panniculitis. Morphea is not associated with systemic symptoms, tends to be distributed in a nonsymmetric pattern, and as opposed to H syndrome, has no associated hypertrichosis, while in plasma cell panniculitis, the most typical clinical finding is tender, erythematous subcutaneous nodules, as opposed to the more diffuse cutaneous lesions that are typical of H syndrome.[8],[9]

Skin thickening and infiltration of the subcutaneous fat are nonspecific findings that may be demonstrated by imaging in various disorders, including myxedema, eosinophilic fasciitis, nephrogenic systemic fibrosis, lymphedema, lipodermatosclerosis, and sclerodermoid graft versus host disease.[8] However, most of these disorders can be easily differentiated from H syndrome based on localization, distribution, and extent of findings as well as by the associated clinical constellation.

Near about 100 cases of H syndrome have been reported till date, with a total of 10 cases being reported from the Indian subcontinent.[9],[10] This is a remarkable number of patients for a relatively novel autosomal recessive disorder, implying that the disease is not rare. Since the disorder has been fully described only recently, it is still misdiagnosed not only due to lack of awareness but also due to the wide spectrum of possible clinical manifestations. It is possible that cases go undiagnosed or are not diagnosed properly because of its overlapping features with other syndromes.

Declaration of patient consent

The authors certify that they have obtained all appropriate patient consent forms. In the form, the patient has given his consent for images and other clinical information to be reported in the journal. The patient understands that name and initial will not be published and due efforts will be made to conceal identity, but anonymity cannot be guaranteed.

Financial support and sponsorship

Nil.

Conflicts of interest

There are no conflicts of interest.

References

1Molho-Pessach V, Agha Z, Aamar S, Glaser B, Doviner V, Hiller N, et al. The H syndrome: A genodermatosis characterized by indurated, hyperpigmented, and hypertrichotic skin with systemic manifestations. J Am Acad Dermatol 2008;59:79-85.
2Molho-Pessach V, Lerer I, Abeliovich D, Agha Z, Abu Libdeh A, Broshtilova V, et al. The H syndrome is caused by mutations in the nucleoside transporter hENT3. Am J Hum Genet 2008;83:529-34.
3Molho-Pessach V, Ramot Y, Camille F, Doviner V, Babay S, Luis SJ, et al. H syndrome: The first 79 patients. J Am Acad Dermatol 2014;70:80-8.
4Prendiville J, Rogers M, Kan A, de Castro F, Wong M, Junker A, et al. Pigmented hypertrichotic dermatosis and insulin dependent diabetes: Manifestations of a unique genetic disorder? Pediatr Dermatol 2007;24:101-7.
5Avitan-Hersh E, Mandel H, Indelman M, Bar-Joseph G, Zlotogorski A, Bergman R, et al. A case of H syndrome showing immunophenotype similarities to Rosai-Dorfman disease. Am J Dermatopathol 2011;33:47-51.
6Doviner V, Maly A, Ne'eman Z, Qawasmi R, Aamar S, Sultan M, et al. H syndrome: Recently defined genodermatosis with distinct histologic features. A morphological, histochemical, immunohistochemical, and ultrastructural study of 10 cases. Am J Dermatopathol 2010;32:118-28.
7Hiller N, Zlotogorski A, Simanovsky N, Ingber A, Ramot Y, Molho-Pessach V, et al. The spectrum of radiological findings in H syndrome. Clin Imaging 2013;37:313-9.
8Rambhia KD, Dongre AM, Khopkar US. Sclerodermoid plaques: A riddle of 'H'. Indian J Dermatol Venereol Leprol 2015;81:327.
9Molho-Pessach V, Varma M, Godbole K, Kamath N, Zlotogorski A. H syndrome – Four new patients from India. Indian J Dermatol Venereol Leprol 2014;80:579.
10Mohanan S, Chandrashekar L, Semple RK, Thappa DM, Rajesh NG, Negi VS, et al. H syndrome with a novel homozygous R134C mutation in SLC29A3 gene. Int J Dermatol 2013;52:820-3.